Variant (rsID / SNP)

rs77396610

rs77396610 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC33. Location: chromosome 15, position 74,625,077. Clinical significance in the table: Likely benign.

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Reference-table entries

CCDC33Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:74625077
Cytoband: 15q24.1
HGVS: NM_025055.5(CCDC33):c.1829C>T (p.Pro610Leu)
Allele change: Missense_P610L

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.